index - Plateforme d’immortalisation MyoLine – CRM

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48 Publications avec texte intégral

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Canine X-linked muscular dystrophy in Japan CXMD J Chromatin DMD CXCR4 Fear response Exondys 51 Gut microbiota CTG⋅CAGn repeat Becker muscular dystrophy Clinical trial candidate screening Duchenne Muscular Dystrophy KLF15 Drisapersen Coculture MSCs Myogenesis Duchenne muscular dystrophy Machine learning LTβR Neuromuscular junction Fibroblast Lymphotoxin-β-receptor Dystrophin Lamin A/C nuclei Flavonoid BAF Gene Therapy Developmental biology Human muscle stem/progenitor cells Human Immortalisation Gene network analysis Acetylcholine receptor subunit epsilon DM1 myoblasts Conjugation Atrial cardiac defects CRISPR/Cas9 Folding-defective proteins Dominant centronuclear myopathy LRP4 Migration Muscle Skeletal muscle CFTR correctors Adeno-associated viral vector BMD Cell Therapy Glucose CMS 3D co-culture Insulin ICU-acquired weakness CLS Computer software Expanded repeats Eteplirsen FSHD Mdx Myotube Emerin Glucocorticoid-induced muscle atrophy Becker muscular dystrophy BMD Duchenne muscular dystrophy DMD miRNA nNOS Autophagy Antisense oligonucleotide Endocytosis MT RNA/DNA Editing Gene therapy ITSN1 CDNA synthesis DiPRO1 Fibrosis Immortalized dystrophic canine myoblast Lamina-associated domain Exon-skipping Adhesion DNM2 Motor neuron FoxO Gel electrophoresis Exon skipping Centronuclear myopathy Alternative splicing Differentiation Allele-specific silencing therapy Cell-penetrating peptide Cell biology HDMD/Dmd-null mice Bile acid CXCL12 Allele-specific silencing Exon Skipping Antisense morpholino DsDNA break repair Human artificial chromosomes Laminographie Dynamin 2 Myotonic dystrophy Autophagosome RNA interference Actin